ライフサイエンスコーパス: chloramphenicol

1 d with ribosome-targeting antibiotics (e.g., chloramphenicol).

2 mia associated with clinical applications of chloramphenicol.

3 o upregulate ceoR promoter activity, as does chloramphenicol.

4 capable of resisting up to 400 microg/mL of chloramphenicol.

5 and the minimum inhibitory concentration of chloramphenicol.

6 bial antibiotics novobiocin, pefloxacin, and chloramphenicol.

7 nthesis had been blocked by spectinomycin or chloramphenicol.

8 its binding is inhibited by the presence of chloramphenicol.

9 ce mechanisms that deactivate tobramycin and chloramphenicol.

10 ng antibiotics: tobramycin, clindamycin, and chloramphenicol.

11 s remain susceptible to either penicillin or chloramphenicol.

12 % were resistant to ampicillin, TMP-SMX, and chloramphenicol.

13 enylephrine 10%, diclophenac 0.1% along with chloramphenicol 0.5% were used preoperatively.Pupil diam

14 5% confidence intervals [CI], 0.35 to 0.87); chloramphenicol, 49% (95% CI, 0.20 to 0.83); trimethopri

15 n, but fewer isolates were nonsusceptible to chloramphenicol (5.7%), meropenem (16.6%), and cefotaxim

16 ethoprim, 20%; piperacillin-tazobactam, 11%; chloramphenicol, 9%; and aminoglycoside, 4%.

17 cin (a cell-wall biosynthesis inhibitor) and chloramphenicol (a protein synthesis inhibitor).

18 Chloramphenicol, a peptidyl transferase inhibitor, affec

19 i cells with the protein synthesis inhibitor chloramphenicol abolished replication blockage, indicati

20 in I (NECI) and analyzed the expression of a chloramphenicol acetyl transferase (CAT) marker gene dri

21 Gel shift analysis and chloramphenicol acetyl transferase (CAT) reporter assays

22 s) or isoform II (60 amino acids) fused to a chloramphenicol acetyl transferase (CAT) reporter demons

23 nd passage was detected by expression of the chloramphenicol acetyl transferase (CAT) reporter gene p

24 fragments thereof to -8 bp, each linked to a chloramphenicol acetyl transferase (CAT) reporter gene.

25 ement into heterologous SV40 promoter (SV40) chloramphenicol acetyl transferase (CAT) vector showed o

26 with the GSTA2 antioxidant response element-chloramphenicol acetyl transferase construct.

27 number of plasmids containing the wild type chloramphenicol acetyl transferase gene rescued from oxi

28 ed a plasmid construct encoding the cDNA for chloramphenicol acetyl transferase modified to contain a

29 Deletion analyses of the promoter and chloramphenicol acetyl transferase reporter gene assays

30 no inhibition of GR-mediated induction of a chloramphenicol acetyl transferase reporter in LMCAT cel

31 olecular mechanism of this effect, we used a chloramphenicol acetyl transferase reporter under the co

32 inserted in the promoter region of the cat (chloramphenicol acetyl transferase) gene on a plasmid.

33 We applied the technique to a model system, chloramphenicol acetyl transferase, to create functional

34 Shear stress activated a human eNOS promoter chloramphenicol acetyl-CoA transferase chimeric construc

35 in PAO1 carried the algD promoter fused to a chloramphenicol acetyl-transferase cartridge (PalgD-cat)

36 corporation of [3H]uridine and a decrease in chloramphenicol acetyltransferase (CAT) activity in a de

37 nic acid capsule genes (hasABC) by measuring chloramphenicol acetyltransferase (CAT) activity in a re

38 Chloramphenicol acetyltransferase (CAT) activity varied

39 Insulin stimulates malic enzyme (ME)-chloramphenicol acetyltransferase (CAT) and collagenase-

40 An ambisense MG coding for chloramphenicol acetyltransferase (CAT) and green fluore

41 n, each cell line was transfected with pRARE-chloramphenicol acetyltransferase (CAT) and treated with

42 to activate both RRE-mediated reporter gene [chloramphenicol acetyltransferase (CAT) and/or gag] expr

43 The analysis of IGRP-chloramphenicol acetyltransferase (CAT) fusion gene expr

44 The analysis of IGRP-chloramphenicol acetyltransferase (CAT) fusion gene expr

45 c and intestinal expressions of the reporter chloramphenicol acetyltransferase (CAT) gene (which subs

46 d transgenic mice in which expression of the chloramphenicol acetyltransferase (CAT) gene is driven b

47 irs was linked to the coding sequence of the chloramphenicol acetyltransferase (CAT) gene.

48 3'UTRs of these transcripts were mapped and chloramphenicol acetyltransferase (CAT) reporter constru

49 r genes and an NFkappaB motif containing the chloramphenicol acetyltransferase (CAT) reporter gene ma

50 ES and Lab-Lb intervening segment fused to a chloramphenicol acetyltransferase (CAT) reporter has bee

51 With newly constructed chloramphenicol acetyltransferase (CAT) reporter vectors

52 oid activation of the promoter attached to a chloramphenicol acetyltransferase (CAT) reporter, but in

53 Using a chloramphenicol acetyltransferase (CAT) target gene, inh

54 A transcriptional fusion of chloramphenicol acetyltransferase (CAT) to the fabB prom

55 ed by a shortened version of intron 1 to the chloramphenicol acetyltransferase (CAT) vector showed th

56 , including green fluorescent protein (GFP), chloramphenicol acetyltransferase (CAT), and luciferase.

57 For that purpose, we decided to use chloramphenicol acetyltransferase (CAT), as chloroplasts

58 the third vector containing a reporter gene, chloramphenicol acetyltransferase (CAT), they were cotra

59 integrated with a mouse mammary tumor virus-chloramphenicol acetyltransferase (MMTV-CAT) reporter, w

60 CHN) resulted in repression of IL-6 promoter chloramphenicol acetyltransferase activity (P < 0.05).

61 The chloramphenicol acetyltransferase activity in all of the

62 was attributed to a decrease in RII promoter-chloramphenicol acetyltransferase activity that was asso

63 The increase in chloramphenicol acetyltransferase activity was also refl

64 kbone fold, which is also similar to that of chloramphenicol acetyltransferase and dihydrolipoyl tran

65 ng partners of an insoluble protein fused to chloramphenicol acetyltransferase by monitoring the surv

66 , and Smads, within the p-560Col7a1 promoter/chloramphenicol acetyltransferase construct, coupled wit

67 emonstrate 32-fold transactivation of an LTR-chloramphenicol acetyltransferase construct.

68 ion at p19, we made a series of p19 promoter chloramphenicol acetyltransferase constructs in which th

69 was examined using the same Col7a1 promoter/chloramphenicol acetyltransferase constructs.

70 disrupted terminal complementarity abolished chloramphenicol acetyltransferase expression and RNA syn

71 to replace the an open reading frame with a chloramphenicol acetyltransferase gene (cat) and a bacmi

72 ssay for (CAG)(n)*(CTG)(n) deletion from the chloramphenicol acetyltransferase gene integrated into t

73 The rates of chloramphenicol acetyltransferase gene transcription dri

74 ch a firefly luciferase gene was linked to a chloramphenicol acetyltransferase gene using a segment o

75 ansformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene, rendering this o

76 ansformed an exthemophilic red alga with the chloramphenicol acetyltransferase gene, rendering this o

77 muscle cells by binding to myocyte-specific chloramphenicol acetyltransferase heptamer elements in t

78 This motif increased the expression of chloramphenicol acetyltransferase in Caco-2 cells treate

79 Fusions of the F-ATPase promoter to chloramphenicol acetyltransferase indicated that pH-depe

80 We found the amount of chloramphenicol acetyltransferase induced by the wild-ty

81 tant to chloramphenicol due to production of chloramphenicol acetyltransferase mediated by catP.

82 ts on VSV in vitro transcription and in vivo chloramphenicol acetyltransferase minigenome replication

83 o reflected at the levels of cytoplasmic RRE-chloramphenicol acetyltransferase mRNAs, indicating that

84 ted with an mouse mammary tumor virus (MMTV) chloramphenicol acetyltransferase reporter (Cat0) synchr

85 of a mutated or deleted residue 1 of a cRNA chloramphenicol acetyltransferase reporter construct, su

86 The minimal promoter sufficient to drive chloramphenicol acetyltransferase reporter gene activity

87 strongly synergized with Tat on Tat-mediated chloramphenicol acetyltransferase reporter gene expressi

88 B expression, the seb promoter fused to the chloramphenicol acetyltransferase reporter gene was intr

89 es were subcloned in front of a promoterless chloramphenicol acetyltransferase reporter gene.

90 gene was cloned, sequenced, and fused to the chloramphenicol acetyltransferase reporter gene.

91 However, in a chloramphenicol acetyltransferase reporter system, only

92 In contrast, when studied in a chloramphenicol acetyltransferase reporter, two promoter

93 polar expression of fluorescent proteins and chloramphenicol acetyltransferase substitutions for the

94 Transfection experiments with OvCAT (chloramphenicol acetyltransferase) reporter constructs d

95 During growth in THB, the reporter activity (chloramphenicol acetyltransferase) was first detected in

96 dition, successful co-expression of GFP with chloramphenicol acetyltransferase, and thioredoxin with

97 in, netilmicin, and tobramycin resistance; a chloramphenicol acetyltransferase, catB8; and gene aadA1

98 hares unexpected similarity to structures of chloramphenicol acetyltransferase, dihydrolipoyl transac

99 mblance of catalysis by the EntF C domain to chloramphenicol acetyltransferase, including an active s

100 lation using three separate reporter assays (chloramphenicol acetyltransferase, luciferase, and red f

101 smid containing a Himar1 transposon encoding chloramphenicol acetyltransferase, mCherry fluorescent p

102 for His-tagged green fluorescent protein and chloramphenicol acetyltransferase, respectively) and wer

103 pment of a method, based on the transport of chloramphenicol acetyltransferase, that allows positive

104 er gene such as green fluorescent protein or chloramphenicol acetyltransferase.

105 e transcriptional activation of the gene for chloramphenicol acetyltransferase.

106 lso possessed the cat2 gene, which encodes a chloramphenicol acetyltransferase.

107 We now report the finding that chloramphenicol administered at reperfusion reduced infa

108 nterestingly, well-known antibiotics such as chloramphenicol also cause a substantial reduction in th

109 ays measuring the efflux from cells of [(3)H]chloramphenicol and [(3)H]tritylimidazole were used.

110 ibited the replication of C. burnetii, while chloramphenicol and ciprofloxacin did not.

111 o traditional first-line antibiotics such as chloramphenicol and co-trimoxazole have significantly de

112 Chloramphenicol and doxycycline resistance evolved smoot

113 as organisms replicating in the presence of chloramphenicol and expressing mCherry.

114 Seven (4%) children with chloramphenicol and five (3%) with placebo had further c

115 A), and brain heart infusion (BHI) agar with chloramphenicol and gentamicin.

116 treptomyces venezuelae ISP5230, affects both chloramphenicol and jadomycin production levels in block

117 owever, our in vitro experiments showed that chloramphenicol and linezolid stall ribosomes at specifi

118 The first broad-spectrum antibiotic chloramphenicol and one of the newest clinically importa

119 Experiments using radiolabeled chloramphenicol and salicylate demonstrated active efflu

120 l agents used to treat Y. pestis, except for chloramphenicol and trimethoprim-sulfamethoxazole.

121 the large ribosomal subunit (macrolides and chloramphenicol) and, intriguingly, the small subunit (d

122 -line antibiotics amoxicillin or penicillin, chloramphenicol, and co-trimoxazole; 68.3% of Gram-negat

123 The prevalence of resistance to ampicillin, chloramphenicol, and cotrimoxazole was 38.11%, with regi

124 slation inhibitors (puromycin, tetracycline, chloramphenicol, and erythromycin) on global transcripti

125 We found that doxycycline, chloramphenicol, and Geneticin (G418) interfered with in

126 o tetracycline, spectinomycin, sulfonamides, chloramphenicol, and gentamicin.

127 y, high swarming motility, low resistance to chloramphenicol, and increased killing of Caenorhabditis

128 sensitivity of DAF binding to inhibition by chloramphenicol, and loss of binding capability to colla

129 parison of the Ki values for oxazolidinones, chloramphenicol, and sparsomycin revealed partial cross-

130 ity, with limits of detection for ofloxacin, chloramphenicol, and streptomycin of 0.3, 0.12, and 0.2

131 solates tested were resistant to ampicillin, chloramphenicol, and trimethoprim-sulfamethoxazole (mult

132 Resistance to at least ampicillin, chloramphenicol, and trimethoprim-sulfamethoxazole (mult

133 solates tested were resistant to ampicillin, chloramphenicol, and trimethoprim-sulfamethoxazole; 4 we

134 a series of jadomycins and between JadX and chloramphenicol, another natural product produced by S.

135 h as aplastic anemia and leukemia induced by chloramphenicol are a major concern.

136 ffinity to efflux transporters (atropine and chloramphenicol) are the likely reasons for these low in

137 Sulfonamide and chloramphenicol ARG levels were largely unaffected by tr

138 nd a short peptide, Crb(CmlA), that requires chloramphenicol as a coinducer of pausing.

139 Using optical sensing of chloramphenicol as a proof of concept, we show here that

140 the lincosamide clindamycin, and a phenicol, chloramphenicol, at resolutions of approximately 3.3 A-3

141 of decreased Salmonella typhi resistance to chloramphenicol, attributed to restricted antibiotic usa

142 ted for sensitive and selective detection of chloramphenicol, based on an indirect competitive enzyme

143 ing of puromycin, while the aromatic ring of chloramphenicol binds to the exit tunnel hydrophobic cre

144 show that CmlA, the beta-hydroxylase of the chloramphenicol biosynthetic pathway, contains a (mu-oxo

145 om Thermus thermophilus suggests a model for chloramphenicol bound to the large subunit of the bacter

146 acteria and treatment of infected cells with chloramphenicol, but not ampicillin, abrogated the induc

147 The ultimate step in chloramphenicol (CAM) biosynthesis is a six-electron oxi

148 Chloramphenicol (Cam) is a broad-spectrum antibiotic use

149 the hydroxyl groups on a "quasi-diffusible" chloramphenicol (Cam) moiety tethered to the evolving li

150 r highly sensitive and specific detection of chloramphenicol (CAP) based on engineered "hot" Au core-

151 sensor is developed for the determination of chloramphenicol (CAP) exploring its direct electron tran

152 ectrochemical biosensor for the detection of chloramphenicol (CAP) in the presence of its analogues h

153 , thiamphenicol (TAP), florfenicol (FFC) and chloramphenicol (CAP) were separated on an Inertsil, C(8

154 In the presence of chloramphenicol (CAP), which freezes translating chlorop

155 cillin [bla(TEM)], streptomycin [strA-strB], chloramphenicol [cat-1], and erythromycin resistance [me

156 Blocking translation with chloramphenicol caused characteristic nucleoid compactio

157 wever, was significantly up-regulated during chloramphenicol challenge and in T. maritima bound in ex

158 sition from exponential to stationary phase, chloramphenicol challenge, and syntrophic coculture with

159 ine E. coli isolates exhibited resistance to chloramphenicol (CHL), an antibiotic whose use in food a

160 ns of MRSA isolates that were susceptible to chloramphenicol, clindamycin, and erythromycin were lowe

161 pneumoniae grows in medium supplemented with chloramphenicol (Cm) when resistant bacteria expressing

162 ons added resistance to ampicillin (Amp) and chloramphenicol (Cm), and the 1,600-bp integron added re

163 filamentous wild-type cells increase as the chloramphenicol concentration increases to 50 and 250 mi

164 g nanoparticles are observed in the cells as chloramphenicol concentration increases, suggesting that

165 oci was induced by amino acid starvation and chloramphenicol, consistent with the proposal that VapB

166 ell density and secretion in the presence of chloramphenicol, constant viability count, the absence o

167 lycan contributions while those treated with chloramphenicol contained a higher percentage of peptido

168 ent, collagen; pretreatment of bacteria with chloramphenicol did not decrease this enhanced adherence

169 glycosides, tetracyclines, lincosamides, and chloramphenicol), DNA synthesis inhibitors (fluoroquinol

170 under selection with single drugs, including chloramphenicol, doxycycline and trimethoprim.

171 rpoB gene, and two strains were resistant to chloramphenicol due to production of chloramphenicol ace

172 east four different antibiotics - isoniazid, chloramphenicol, erythromycin and tetracycline.

173 We assigned 163 children to receive chloramphenicol eye drops and 163 to receive placebo eye

174 -blind trial to compare the effectiveness of chloramphenicol eye drops with placebo in children with

175 II was potentially influenced by the use of chloramphenicol for the treatment of iNTS disease.

176 Efficient production of chloramphenicol from the free arylamine precursor sugges

177 In addition to the chloramphenicol gene, a second gene neo was introduced f

178 is reaction was insensitive to 100 microg/ml chloramphenicol, gentamycin, paromomycin, lincomycin, hy

179 Nine children were lost to follow-up (one in chloramphenicol group; eight in placebo group).

180 Swarming on agar to which chloramphenicol had been added suggested that protein sy

181 The context-specific action of chloramphenicol illuminates the operation of the mechani

182 on oxygenation of the arylamine precursor of chloramphenicol in a nonribosomal peptide synthetase (NR

183 al methods for detection and quantitation of chloramphenicol in blood serum and foodstuffs arse highl

184 istic insights into high-level resistance to chloramphenicol in C. jejuni, using integrated genomic a

185 Our structure of chloramphenicol in complex with the 70S ribosome from Th

186 r the cat gene that determines resistance to chloramphenicol in Escherichia coli.

187 c aptasensor was successfully used to detect chloramphenicol in milk and serum with LODs of 697 and 6

188 e, trimethoprim, macroline, beta-lactams and chloramphenicol in the aquatic ecosystems.

189 Bacterial clones resistant to chloramphenicol in vivo were recovered from the livers o

190 he thermal degradation of a veterinary drug, chloramphenicol, in model solutions (water), as well as

191 col concentration increases, suggesting that chloramphenicol increases membrane permeability and poro

192 bition of mitochondrial protein synthesis by chloramphenicol increases the susceptibility of endothel

193 reviously observed effects of rifampicin and chloramphenicol indicate that transcription and translat

194 olerance of PSII was completely abolished by chloramphenicol, indicating that the acclimation mechani

195 were heat or formalin killed or treated with chloramphenicol, indicating that the TLR2 agonist activi

196 However, the mechanism underlying chloramphenicol-induced leukemogenesis is not known.

197 owed that transcription is necessary for the chloramphenicol-induced nucleoid compaction.

198 staphylococcal enterotoxin B, we found that chloramphenicol induces the differentiation of activated

199 ses to 50 and 250 microg/mL, suggesting that chloramphenicol induces the filamentation.

200 ransferase activity in all of the strains is chloramphenicol inducible.

201 Chloramphenicol inhibited the activation-induced cell de

202 s as infected cells treated with rifampin or chloramphenicol, inhibitors of bacterial RNA and protein

203 Chloramphenicol is a broad-spectrum antibiotic used for

204 Chloramphenicol is an inhibitor of mitochondrial protein

205 Resistance to both gentamicin and chloramphenicol is encoded on pGNS-BAC, permitting selec

206 l step in the biosynthesis of the antibiotic chloramphenicol is the oxidation of an aryl-amine substr

207 chloroplasts are particularly vulnerable to chloramphenicol lethal effects.

208 of amoxicillin with clavulanate, ampicillin, chloramphenicol, metronidazole, and penicillin were dete

209 ll B. anthracis isolates were susceptible to chloramphenicol (MICs, <or=8 microg/ml), ciprofloxacin (

210 ur application to aptamers for streptomycin, chloramphenicol, neomycin B and ATP identifies 37 candid

211 cross-resistance between oxazolidinones and chloramphenicol; no cross-resistance was observed with s

212 8 restored the sensitivity to ampicillin and chloramphenicol of a Mycobacterium smegmatis mutant lack

213 of the following comparator drugs: cefixime, chloramphenicol, ofloxacin, or ceftriaxone.

214 By investigating the effects of chloramphenicol on the activation of mouse T cells stimu

215 ed resistance or decreased susceptibility to chloramphenicol or ciprofloxacin.

216 i and Staphylococcus aureus is suppressed by chloramphenicol or erythromycin, the susceptibility of t

217 uced by the addition of ribosome inhibitors (chloramphenicol or streptomycin) that indirectly constra

218 In the presence of doxycycline, chloramphenicol, or G418, the Sec-containing form of TR1

219 Isolates were generally susceptible to chloramphenicol, penicillin and rifampin, but almost 60%

220 J774.16 cells were treated with 8 microg of chloramphenicol per ml, 4 microg of tetracycline per ml,

221 ded proteins or mitochondrial respiration in chloramphenicol-perfused hearts, and hypothesized that t

222 Arresting translation elongation with chloramphenicol quickly inhibits RNase E cleavage downst

223 racellular pYV(+) Y. pseudotuberculosis with chloramphenicol reduced apoptosis, indicating that the d

224 We also showed that chloramphenicol reduced infarct size in an open chest ra

225 chemically suppressing ppGpp synthesis with chloramphenicol relieves inhibition of DNA replication i

226 The biosynthesis of chloramphenicol requires a beta-hydroxylation tailoring

227 various H. pylori strains by insertion of a chloramphenicol resistance cassette into lpxEHP and exam

228 constructed by replacing the P6 gene with a chloramphenicol resistance cassette.

229 previously employed, using tetracycline and chloramphenicol resistance cassettes, and non-polar stra

230 In contrast, the chloramphenicol resistance gene catII was more frequentl

231 A chloramphenicol resistance gene, a modified lux operon f

232 WGS data revealed the integration of a chloramphenicol resistance gene, the deletion of the end

233 the fla operon promoter and a staphylococcal chloramphenicol resistance gene, was constructed to help

234 ria and the inducible cmlA gene that confers chloramphenicol resistance in Pseudomonas spp.

235 resulted in the introduction of a selectable chloramphenicol resistance marker into the chromosome.

236 containing transposon-based tetracycline and chloramphenicol resistance markers were combined to allo

237 omycin resistance occurred in 132 (37%), and chloramphenicol resistance occurred in 33 (9%).

238 Chloramphenicol resistance was due in part to the dissem

239 In filter matings, chloramphenicol resistance was observed to transfer from

240 Bacteria with target genes expressing chloramphenicol resistance, penicillin resistance, or gy

241 n the plasmid were selected according to the chloramphenicol resistance.

242 and > 50 compounds were tested for promoting chloramphenicol resistance.

243 ml), 4/242 isolates tested were resistant to chloramphenicol (resistance breakpoint >/= 32 mug/ml), 1

244 individually engineered into a plasmid-borne chloramphenicol-resistance (cat) gene driven by the lac

245 A chloramphenicol-resistance (Cm(r)) reporter is used to s

246 erences in protein yields when cloned from a chloramphenicol resistant vector into an identical vecto

247 tumefaciens strains C58, A136, and BG53 are chloramphenicol resistant, and each contains the catB ge

248 l cat gene; induced lysogens survive and are chloramphenicol resistant.

249 + variants in the inoculum by constructing a chloramphenicol-resistant (Cm(r)) strain and following C

250 Penicillin-resistant and chloramphenicol-resistant bacteria are a considerable th

251 meningitis caused by penicillin-resistant or chloramphenicol-resistant bacteria.

252 by measuring the production of Lac-deficient chloramphenicol-resistant bacterial progeny.

253 s, cells can survive the disruption and form chloramphenicol-resistant colonies.

254 hat relies on the folate-dependent growth of chloramphenicol-resistant Lactobacillus casei subspecies

255 etracycline-, ampicillin-, erythromycin-, or chloramphenicol-resistant oral and urinary bacteria as c

256 Short-term exposure of cells to chloramphenicol results in increased activities in both

257 of transertion by the translation inhibitor chloramphenicol results in nucleoid condensation due to

258 tivities, but long-term exposure of cells to chloramphenicol results in selective loss of the soluble

259 MPCs were estimated for tobramycin, chloramphenicol, rifampicin, penicillin, vancomycin, and

260 placebo compared with 140 (86%) of 162 with chloramphenicol (risk difference 3.8%, 95% CI -4.1% to 1

261 al point mutations that confer resistance to chloramphenicol showed no tendency to change in frequenc

262 presence of two antibiotics (ampicillin and chloramphenicol) so that the coculture can survive in an

263 Structures of anisomycin, chloramphenicol, sparsomycin, blasticidin S, and virgini

264 Conjugation of a chloramphenicol-specific DNA aptamer to the protein shel

265 Neither the oxazolidinones nor chloramphenicol stimulated misincorporation of amino aci

266 The first was resistance to ampicillin, chloramphenicol, streptomycin, sulfamethoxazole, and tet

267 s showed multidrug resistance to ampicillin, chloramphenicol, streptomycin, sulfamethoxazole-sulfisox

268 ental isolates were resistant to ampicillin, chloramphenicol, streptomycin, sulfisoxazole, and tetrac

269 first component of the study, pigs received chloramphenicol succinate (CAPS) (an agent that purporte

270 ty to the translational elongation inhibitor chloramphenicol suggesting a link between translational

271 rains were cross-resistant to anisomycin and chloramphenicol, suggesting that Tcin targets the peptid

272 that encodes genes that confer resistance to chloramphenicol, sulphamethoxazole, trimethoprim and str

273 of four antibiotics (ampicillin, cefalexin, chloramphenicol, tetracycline) and their combinations on

274 ]) were associated with nonsusceptibility to chloramphenicol, tetracycline, and co-trimoxazole.

275 reatment with translation inhibitors such as chloramphenicol, tetracycline, and streptomycin gather p

276 h is preceded by elongation, is inhibited by chloramphenicol, tetracycline, or rifampin, and is depen

277 eta-lactams, aminoglycosides, glycopeptides, chloramphenicols, tetracycline, macrolides, trimethoprim

278 In the absence of chloramphenicol, the sandwich structure of aptasensor fo

279 ly and clinically relevant concentrations of chloramphenicol through analyte-mediated inner filtering

280 h peptidyl moieties as well as conjugates of chloramphenicol to either nucleotide groups or pyrene ha

281 Chloramphenicol transacetylase transcriptional fusions i

282 mitochondrial blockers of protein synthesis (chloramphenicol), transcription and replication (ethidiu

283 inant adenoviruses carrying ectopic E2E-CAT (chloramphenicol transferase) reporter genes with mutatio

284 A concentration-dependent inhibition of chloramphenicol transport was observed with imidazole de

285 not p53, c-myc, and CDC25A, was detected in chloramphenicol-treated activated T cells, which may rel

286 the results showed that gentamicin-killed or chloramphenicol-treated bacteria did not induce DNA frag

287 In contrast, chloramphenicol treatment of macrophages infected at mul

288 flux gene cluster that confers resistance to chloramphenicol, trimethoprim, and ciprofloxacin has bee

289 Two extraction strategies for albendazole, chloramphenicol, trimethoprim, enrofloxacin, oxitetracyc

290 ate-bounded method for the following agents: chloramphenicol, trimethoprim-sulfamethoxazole, ciproflo

291 illin, cefotaxime, cefuroxime, erythromycin, chloramphenicol, vancomycin, quinupristin-dalfopristin (

292 (+)-Chloramphenicol was generated in 4 steps from commercial

293 iologic studies, whereas Sabouraud agar with chloramphenicol was the medium for fungal studies.

294 erogroup and MIC to penicillin, rifampin and chloramphenicol were determined.

295 in), peptides (bacitracin, cycloserine), and chloramphenicol were found to differ significantly.

296 metry, the resulting degradation products of chloramphenicol were identified in water, spiked and inc

297 terial infection, 0.3% norfloxacin or 0.25 % chloramphenicol were prescribed.

298 Most of the ivi clones were sensitive to chloramphenicol when grown in vitro.

299 e aortic endothelial cells were treated with chloramphenicol, which resulted in a decreased ratio of

300 aptasensor exhibited high selectivity toward chloramphenicol with a limit of detection as low as 451

301 The patient was treated with intravenous chloramphenicol without success.